Medical%20Virology%20Immunology - PowerPoint PPT Presentation

Title: Medical%20Virology%20Immunology


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Medical Virology Immunology

• Dr. Sameer Naji, MB, BCh, PhD (UK)
• Dean Assistant
• Head of Basic Medical Sciences Dept.
• Faculty of Medicine
• The Hashemite University

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Human blood cells
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Phases of immune responses
Microbe
Naïve T cells
Effector T cells
Memory T cells
Naïve B cells
Memory B cells
Plasma cells
Rapid protection
Long-lived protection
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Immunity to microbes general principles

• Host response to virus infection
• The bodys defense mechanisms to virus infection
  are of two types 1) Non specific 2)
  Specific
• Defense against infections is mediated by the
  early reactions of innate immunity and the later
  responses of adaptive immunity
• The innate immune response controls infection
  long enough for adaptive responses to kick in,
  and can often eradicate the infection
• Many pathogenic microbes resist innate immunity
• Adaptive immunity is able to combat these
  microbes -- the lymphocyte expansion that is
  characteristic of adaptive immunity helps to keep
  pace with rapidly dividing microbes specialized
  immune responses are better able to deal with
  diverse microbes

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Immunity to microbes general principles

• The immune system is specialized to generate
  different effector mechanisms for different types
  of microbes
• Extracellular microbes antibodies, phagocytes
  TH1
• Intracellular microbes phagocytes TH1 CTLs

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Body Defense Mechanisms

• Non specific defense mechanisms (Innate
  immunity)
• The body has defenses which are not
  specifically directed at particular infectious
  agents, but which serve as non-immunological
  barriers to infection
• 1) Skin- an effective and impermeable barrier
  unless breached by injury, disease, etc
• 2) Respiratory tract- upwards flow of mucus by
  ciliated epithelium removes virus particles, to
  prevent invasion of the lower respiratory tract.
• 3) Gastrointestinal tract- stomach acid
  inactivates acid-labile viruses. Bile (lyses
  enveloped viruses), movement of intestinal
  contents and uptake of virus by lymphoid tissue
  all aid elimination of ingested viruses.
• 4) Urinary tract- flow of urine exerts a
  protective flushing effect.
• 5) Conjunctiva- tears flush viruses from the
  eye.

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Body Defense Mechanisms

• 6) Phagocytosis- an important defense mechanism
  in bacterial infection and in virus infections
  also invading viruses- like bacteria- are
  ingested by two types of scavenger cell
• a) neutrophil polymorphonuclear leukocytes
  (PMN).
• b) macrophages (or mononuclear cells of the
  reticuloendothelial
• system)- of two types
• 1) free macrophages in lung
  alveoli, peritoneum.
• 2) fixed macrophages in lymph nodes, spleen,
  liver (Kupffer
• cells),
  connective tissue (histiocytes) and CNS
  (microglia).
• Phagocytosis is enhanced by antibody (a
  specific immune mechanism) and complement this
  effect is known as opsonization.
• Macrophages activated by cytokines
  released by T lymphocytes a specific immune
  mechanism) have increased phagocytic activity and
  are attracted by chemotaxis to the site of
  infection.

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Body Defense Mechanisms

• Cytokines
• Cytokines are small protein molecules released by
  many cells, including lymphocytes and
  macrophages they function as signals or
  mediators to activate, modulate and control the
  immune responses (and other activities) of cells.
• There are numerous cytokines, e.g. interferons,
  interleukins and tumour necrosis factor many act
  sequentially and interact with other cytokines.
• In addition to their role in the immune response,
  some have physiological functions such as tissue
  repair, differentiation and signaling activity in
  the CNS.

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Interferon as Body Defense Mechanism

• Small protein produced by certain cells
• Alpha interferon- lymphocytes macrophages
• Beta interferon fibroblasts epithelial cells
• Gamma interferon T cells (specific immunity)
• Produced in response to viruses, RNA, immune
  products, and various antigens
• Bind to cell surfaces and induce expression of
  antiviral proteins
• Inhibit expression of cancer genes
• Mechanism of action of Interferons
• Induction of the following enzymes
• 1) a protein kinase which inhibits protein
  synthesis
• 2) an oligo-adenylate synthase which leads to
  degradation of viral mRNA
• 3) a phosphodiesterase which inhibit t-RNA
• The action of these enzymes leads to an
  inhibition of translation

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Interferon
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Body Defense Mechanisms

• Specific (Adaptive immunity) defense mechanisms
• Immunological responses are of two types
• 1) Humoral- main effect is neutralization of
  viruses
• responsible for protective immunity.
• 2) cellular- main effect is localization of
  lesions
• kills virus-infected cells.

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Body Defense Mechanisms

• Humoral (antibody) response
• Like other infectious agents, viruses induce
  production of antibodies in the blood. Antibodies
  are
• 1) Immunoglobulins- proteins which react
  specifically with antigens- which are also
  usually proteins and of which the most important
  in protective immunity are those on the surface
  of virus particles.
• 2) Plasma cells- formed when B-lymphocytes are
  activated by encounter with antigen.
  B-lymphocytes have immunoglobulin on their
  surface, which acts as receptors for virus
  antigen. Helper T cells contribute to the
  differentiation of B- cells into plasma cells.

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Antibodies

• Immunoglobulin (Ig)
• A large Y-shaped protein
• Consists of 4 polypeptide chains
• Contains 2 identical fragments (Fab) with ends
  that bind to specific antigen
• Fc binds to self

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Body Defense Mechanisms

• Humoral (antibody) response
• Three immunoglobulins are mainly responsible for
  humoral immunity in virus infections
• 1) IgM- the earliest antibody produced appears
  at a variable interval after exposure, depending
  on the virus, incubation period, dose and route
  of transmission persists for about 4-6 weeks,
  sometimes longer a pentamer of five IgG
  molecules.
• 2) IgG- formed later than IgM but persists long
  term, often for years responsible for immunity
  to reinfection.
• 3) IgA- a dimeric molecule, found in body
  secretions (as well as blood), i.e. saliva,
  respiratory secretions, tears and intestinal
  contents the main antibody involved in immunity
  to respiratory viruses and in gut immunity
  associated with enteric virus infection
  secretory IgA acquires a carbohydrate transport
  piece in extracellular fluids that is absent
  from serum IgA.

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Body Defense Mechanisms

• Cell-mediated immunity
• Cellular immunity plays an important part in the
  response of the body to viruses.
• Children with congenital deficiency of cellular
  immunity are abnormally susceptible to virus
  infection and often (although not always) develop
  unusually severe disease those with humoral
  immune deficiency, on the other hand, respond
  normally to virus infections.
• Cell-mediated immunity is the mechanism for the
  elimination of virus-infected cells- and
  therefore virus- from the body.
• T- or thymus-dependent lymphocytes are the
  principal cells involved in this.
• There are two main types
• 1) CD4-positive helper T-cells 2) CD8-positive
  cytotoxic T-cells

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Antigen processing and presentation
Epitope
MHC Distinguish between self and nonself MHC I
all cells MHCII Macrophages, dendritic cells,
some T and B cells
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Body Defense Mechanisms

• Cell-mediated immunity(continue)
• 1) CD4-positive helper T-cells- carry CD4
  receptors as markers on the their surface. The
  most important cells in the cellular response,
  they liberate cytokines that activate and
  modulate cellular immune responses. They require
  MHC (Major Histocompatibility Complex) class II
  antigens to be presented in association with the
  target antigen for their activation. They also
  interact with B-lymphocytes for antibody
  production.
• 2) CD8-positive cytotoxic T-cells- carry the
  marker CD8 receptor on their surface and are MHC
  Class I antigen-restricted. They lyse target
  cells such as virus-infected cells and tumour
  cells the main mechanism for elimination of
  virus-infected cells from the body also release
  cytokines.
• Suppressor function note that both CD4 and CD8
  cells can suppress as well as activate the
  cellular response.
• Virus is recognized as antigen by helper T-cells
  when presented by a macrophage or dendritic cell
  (found in lymph nodes and skin) acting as an
  antigen-presenting cell recognition is dependent
  on MHC Class II antigens.

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T-cell response
CD4 coreceptor
B-cell proliferation and differentiation
CD8 coreceptor
Specific antiviral antibodies bind circulating
virus
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Cytotoxic T cells
Perforins Granzymes
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Principal mechanisms of defense against microbes
Antibodies
Phagocytes
T cells (CTLs)
(may work with
antibodies, T cells)
All microbes
Intracellular microbes, esp. viruses
All microbes
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Properties and roles of memory cells

• Survive even after infection is cleared
• Numbers more than naïve cells
• Respond to antigen challenge (recall) more
  rapidly than do naïve cells
• Memory T cells migrate to tissues, some live in
  mucosal tissues and skin
• Memory B cells produce high affinity antibodies
• Provide rapid protection against recurrent or
  persistent infections
• Goal of vaccination is to induce effective memory
  

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Specialization of immune responses to microbes
Effector mechanism
Type of microbe
Adaptive immune response
Extracellular microbe (bacteria, viruses)
Endocytosed antigen stimulates CD4 helper T
cells (TH1, TH17) --gt antibody, inflammation
Neutralization, phagocytosis
Intracellular microbe in phagocytes
Antigen in vesicles or cytosol --gt CD4, CD8 T
cells
IFN-g activates phagocytes killing of infected
cells
Intracellular microbe in non-phagocytic cell
(virus)
Antigen in cytosol --gt CD8 CTLs
Killing of infected cells
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Cell-mediated immunity against intracellular
microbes
CD4 T cells make phagocytes better killers of
microbes
CTLs eliminate the reservoir of infection
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CD4 and CD8 T cells cooperate in cell-mediated
immunity against intracellular microbes
CD4 T cells help to kill microbes in vesicles
of phagocytes
CD8 CTLs kill microbes that have escaped into
the cytoplasm
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Innate and adaptive immunity to viruses
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Innate and adaptive immune responses in viral
infections
Innate immunity
Adaptive immunity
Antibody
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Roles of antibodies and CTLs in adaptive immunity
to viruses

• Antibodies neutralize viruses and prevent
  infection
• Block infectious virus early in course of
  infection (before entering cells) or after
  release from infected cells (prevents
  cell-to-cell spread)
• CTLs kill infected cells and eradicate reservoirs
  of established infection
• In some latent viral infections (EBV, CMV), CTLs
  control but do not eradicate the infection
  defective T cell immunity leads to reactivation
  of the virus (in HIV, immunosuppression caused by
  leukemias, treatment for graft rejection)

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Immune evasion by viruses

• Antigenic variation
• Influenza, HIV, rhinovirus
• Inhibition of the class I MHC antigen processing
  pathway
• Different viruses use different mechanisms
• NK cells are the host adaptation for killing
  class I MHC-negative infected cells
• Production of immune modulators
• Soluble cytokine receptors may act as decoys
  and block actions of cytokines (poxviruses)
• Immunosuppressive cytokines, e.g. IL-10 (EBV)
• Infection of immune cells
• HIV

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Efficacy of vaccines

• Vaccines have been useful for generating
  protective antibodies, but so far, not for
  generating effective cell-mediated immunity
• Vaccines work best against microbes that
• Do not vary their antigens
• Do not have animal reservoirs
• Do not establish latent infection within host
  cells
• Do not interfere with the host immune response